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THE EFFECT OF AROMATHERAPY FOOT BATHS ON CANCER PATIENTS

THE EFFECT OF AROMATHERAPY FOOT BATHS ON PAIN, SLEEP QUALITY, AND FATIGUE IN CANCER PATIENTS: A RANDOMIZED CONTROLLED TRIAL

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07721168
Acronym
AROMA-FOOTBATH
Enrollment
70
Registered
2026-07-22
Start date
2026-08-01
Completion date
2026-12-01
Last updated
2026-07-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients Diagnosed With Cancer

Keywords

Aromatherapy, Foot bath, Pain, Fatigue, Sleep quality

Brief summary

The goal of this randomised clinical trial is to evaluate the effects of aromatherapy-infused foot baths on pain, sleep quality, and fatigue in cancer patients. The main question\[s\] it aims to answer are: * Is an aromatherapy foot bath effective in reducing pain in cancer patients? * Is an aromatherapy foot bath effective in improving sleep quality in cancer patients? * Is an aromatherapy foot bath effective in reducing fatigue in cancer patients? The experimental group will receive a total of 5 sessions of aromatherapy foot baths, each lasting 20 minutes per day for 5 days, administered by the researcher. The control group will receive only routine care without any treatment. Before and after all treatments are completed, participants will be given and asked to complete the Hirai Cancer Fatigue Scale, the Pittsburgh Sleep Quality Index (PSQI), and the Numerical Pain Scale. The pain, fatigue, and sleep quality scores of the experimental and control groups will then be compared.

Interventions

OTHERAromatherapy

The experimental group will receive a foot bath treatment containing aromatherapy for 5 days administered by the researcher. A foot bath device will be used. Lavender essential oil will be added to the water as aromatherapy. Then, the researcher will administer a foot bath to the patient using this water.

Sponsors

Ankara Yildirim Beyazıt University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients over 18 years of age, * Conscious (Glasgow coma scale: 15 points) * No diagnosis of mental illness * No respiratory distress * No diagnosis of respiratory system disorder * Patients who agree to participate in the study

Exclusion criteria

* Patients under 18 years of age, * Patients with a Glasgow Coma Scale score below 15 points, * Patients with a diagnosis of mental illness, * Patients with respiratory distress, * Patients with a diagnosis of respiratory system disease, * Patients with hemiplegia or paraplegia, * Patients who refused to participate in the study.

Design outcomes

Primary

MeasureTime frameDescription
Hirai Cancer Fatigue ScaleBaseline and day 5The scale has a minimum score of 15 and a maximum score of 75. Higher scores indicate increased fatigue, while lower scores indicate decreased fatigue.
Numerical Pain ScaleBaseline and day 5Participants will be asked to rate the intensity of their pain on a scale of 0 (no pain) to 10 (most severe pain). A higher score indicates increasing pain.
Pittsburgh Sleep Quality IndexBaseline and day 5The total score ranges from 0 to 21. A total score higher than 5 indicates poor sleep quality.

Contacts

CONTACTErdal Ceylan
erdalceylan@aybu.edu.tr+905362323599
PRINCIPAL_INVESTIGATORSemra Gündoğdu

Ankara Yildirim Beyazıt University

STUDY_DIRECTORErdal Ceylan

Ankara Yildirim Beyazıt University

STUDY_CHAIRAhmet Özgen Yıldırım

Ankara Etlik City Hospital

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 23, 2026